| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:118014017-118014221 | Common:2; Rare:111 | ||||
| chr2:118088346-118088509 | Common:1; Rare:50 | ||||
| chr2:119366776-119367059 | Common:1; Rare:86 | ||||
| chr2:119367119-119367303 | Rare:40 | ||||
| chr2:119679072-119679219 | Common:3; Rare:46 | ||||
| chr2:120012889-120013091 | Common:2; Rare:78 | ||||
| chr2:121530589-121530880 | Common:7; Rare:115 | ||||
| chr2:121649415-121649645 | Common:2; Rare:66 | ||||
| chr2:121736745-121737229 | Common:5; Rare:197 | ||||
| chr2:126655782-126655936 | Rare:49 | ||||
| chr2:126655941-126656311 | Common:1; Rare:98; Clinvar:2 | ||||
| chr2:127294077-127294212 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387962-127388198 | Common:3; Rare:100 | ||||
| chr2:127811139-127811241 | Rare:31 | ||||
| chr2:127858107-127858205 | Rare:51 |